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dc.contributor.authorMcCloskey, Douglas
dc.contributor.authorPalsson, Bernhard O.
dc.contributor.authorYang, Jason Hung-Ying
dc.contributor.authorSaluja, Prerna Bhargava
dc.contributor.authorMao, Ning
dc.contributor.authorCollins, James J.
dc.date.accessioned2019-01-24T21:55:37Z
dc.date.available2019-01-24T21:55:37Z
dc.date.issued2017-12
dc.identifier.issn1931-3128
dc.identifier.urihttp://hdl.handle.net/1721.1/120132
dc.description.abstractBactericidal antibiotics alter microbial metabolism as part of their lethality and can damage mitochondria in mammalian cells. In addition, antibiotic susceptibility is sensitive to extracellular metabolites, but it remains unknown whether metabolites present at an infection site can affect either treatment efficacy or immune function. Here, we quantify local metabolic changes in the host microenvironment following antibiotic treatment for a peritoneal Escherichia coli infection. Antibiotic treatment elicits microbiome-independent changes in local metabolites, but not those distal to the infection site, by acting directly on host cells. The metabolites induced during treatment, such as AMP, reduce antibiotic efficacy and enhance phagocytic killing. Moreover, antibiotic treatment impairs immune function by inhibiting respiratory activity in immune cells. Collectively, these results highlight the immunomodulatory potential of antibiotics and reveal the local metabolic microenvironment to be an important determinant of infection resolution. Antibiotic susceptibility is sensitive to metabolites, but how this affects in vivo treatment efficacy remains unexplored. Yang, Bhargava et al. characterize antibiotic-induced changes to the metabolic environment during infection and find that direct actions of antibiotics on host cells induce metabolites that impair drug efficacy and enhance phagocytic activity.en_US
dc.description.sponsorshipUnited States. Defense Threat Reduction Agency (Grant HDTRA1-15-1-0051)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant U01AI124316)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant K99GM118907)en_US
dc.description.sponsorshipNovo Nordisk Foundation (Grant NNF16CC0021858)en_US
dc.description.sponsorshipPaul G. Allen Frontiers Groupen_US
dc.description.sponsorshipWyss Institute for Biologically Inspired Engineeringen_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.CHOM.2017.10.020en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleAntibiotic-Induced Changes to the Host Metabolic Environment Inhibit Drug Efficacy and Alter Immune Functionen_US
dc.typeArticleen_US
dc.identifier.citationYang, Jason H., Prerna Bhargava, Douglas McCloskey, Ning Mao, Bernhard O. Palsson, and James J. Collins. “Antibiotic-Induced Changes to the Host Metabolic Environment Inhibit Drug Efficacy and Alter Immune Function.” Cell Host & Microbe 22, no. 6 (December 2017): 757–765.e3. © 2017 Elsevier Inc.en_US
dc.contributor.departmentInstitute for Medical Engineering and Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorYang, Jason Hung-Ying
dc.contributor.mitauthorSaluja, Prerna Bhargava
dc.contributor.mitauthorMao, Ning
dc.contributor.mitauthorCollins, James J.
dc.relation.journalCell Host & Microbeen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-12-19T16:08:29Z
dspace.orderedauthorsYang, Jason H.; Bhargava, Prerna; McCloskey, Douglas; Mao, Ning; Palsson, Bernhard O.; Collins, James J.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0921-4657
dc.identifier.orcidhttps://orcid.org/0000-0002-5560-8246
mit.licensePUBLISHER_CCen_US


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